Talha Khawaja M, Anker Stefan D, Butler Javed
Department of Medicine, University of Mississippi Medical Center, Jackson, MS, USA.
Department of Cardiology (CVK), and Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Center for Cardiovascular Research (DZHK) Partner Site Berlin, Charité Universitätsmedizin Berlin, Berlin, Germany.
Int J Heart Fail. 2023 Mar 13;5(2):82-90. doi: 10.36628/ijhf.2022.0030. eCollection 2023 Apr.
Sodium-glucose co-transporter 2 (SGLT-2) inhibitors are the latest addition to guideline-directed medical therapy in heart failure (HF) with reduced ejection fraction with recent trials suggesting a significant reduction in adverse cardiovascular outcomes in patients with HF with mildly reduced and preserved ejection fraction. SGLT-2 inhibitors have evolved as metabolic drugs due to their multi-system effects and are indicated for the management of HF across the ejection fraction spectrum, type 2 diabetes, and chronic kidney disease. There is ongoing research to explore the mechanistic effects of SGLT-2 inhibitors in HF and to evaluate their use in worsening HF and after myocardial infarction. This review focuses on the evidence for SGLT-2 inhibitors from type 2 diabetes cardiovascular outcome and primary HF trials and discusses ongoing research related to their use in cardiovascular disease.
钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂是射血分数降低的心力衰竭(HF)指南指导药物治疗中的最新药物,近期试验表明,轻度射血分数降低和射血分数保留的HF患者的不良心血管结局显著减少。由于其多系统效应,SGLT-2抑制剂已发展成为代谢药物,适用于整个射血分数范围的HF、2型糖尿病和慢性肾脏病的管理。目前正在进行研究,以探索SGLT-2抑制剂在HF中的作用机制,并评估其在HF恶化和心肌梗死后的应用。本综述重点关注2型糖尿病心血管结局和原发性HF试验中SGLT-2抑制剂的证据,并讨论与其在心血管疾病中的应用相关的正在进行的研究。